ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.493G>A (p.Asp165Asn)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004015877 SCV004826176 uncertain significance Fabry disease 2023-05-31 criteria provided, single submitter clinical testing

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